Showing
1 - 10
results of
10
Skip to content
VuFind
Log in
Library Catalogue Plus
Library
Subject guides
Databases
Referencing
Catalogue
Articles Plus
Keyword
Title
Author
Subject
Find
Advanced Search
Search Results - Koçak Eker, Hatice
Search Results - Koçak Eker, Hatice
Showing
1 - 10
results of
10
Refine Results
Sort
Relevance
Date Descending
Author
Title
1
Loading…
Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia
by
Kiraz, Aslıhan
,
Sezer, Ozlem
,
Alemdar, Adem
,
Canbek, Sezin
,
Duman, Nilgun
,
Bisgin, Atıl
,
Cora, Tulin
,
Ruhi, Hatice Ilgın
,
Ergoren, Mahmut Cerkez
,
Geçkinli, Bilgen Bilge
,
Sag, Sebnem Ozemri
,
Gözden, Hilmi Erdem
,
Oz, Ozlem
,
Altıntaş, Zuhal Mert
,
Yalcıntepe, Sinem
,
Keskin, Adem
,
Tak, Ayşegül Yabacı
,
Paskal, Şeyma Aktaş
,
Yürekli, Uğur Fahri
,
Demirtas, Mercan
,
Evren, Emine Unal
,
Hanta, Abdullah
,
Başdemirci, Müşerref
,
Suer, Kaya
,
Balta, Burhan
,
Kocak, Nadir
,
Karabulut, Halil Gürhan
,
Cobanogulları, Havva
,
Ateş, Esra Arslan
,
Bozdoğan, Sevcan Tuğ
,
Eker, Damla
,
Ekinci, Sadiye
,
Nergiz, Süleyman
,
Tuncalı, Timur
,
Yagbasan, Serap
,
Alavanda, Ceren
,
Kutlay, Nuket Yurur
,
Evren, Hakan
,
Erdoğan, Murat
,
Altıner, Sule
,
Sanlidag, Tamer
,
Gonen, Gizem Akıncı
,
Vicdan, Arzu
,
Eras, Nazan
,
Eker, Hatice Koçak
,
Balasar, Ozgür
,
Tuncel, Gulten
,
Dundar, Munis
,
Gurkan, Hakan
,
Temel, Sehime Gulsun
Published in
Journal of medical virology
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
2
Loading…
A homozygous mutation in the POMT2 gene in four siblings with limb-girdle muscular dystrophy 2N
by
Yıldırım, Miraç
,
Koçak Eker, Hatice
,
Doğan, Melih Timuçin
Published in
Turkish archives of pediatrics
Get full text
Items that cite this one
Article
Save to List
Saved in:
3
Loading…
Clinical manifestations of 11 children with fronto-ocular syndrome (FOS): a case series
by
Eker, Hatice Koçak
Published in
Child's nervous system
Get full text
Items that this one cites
Article
Save to List
Saved in:
4
Loading…
Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability
by
Duan, Ruizhi
,
Hijazi, Hadia
,
Gulec, Elif Yilmaz
,
Eker, Hatice Koçak
,
Costa, Silvia R.
,
Sahin, Yavuz
,
Ocak, Zeynep
,
Isikay, Sedat
,
Ozalp, Ozge
,
Bozdogan, Sevcan
,
Aslan, Huseyin
,
Elcioglu, Nursel
,
Bertola, Débora R.
,
Gezdirici, Alper
,
Du, Haowei
,
Fatih, Jawid M.
,
Grochowski, Christopher M.
,
Akay, Gulsen
,
Jhangiani, Shalini N.
,
Karaca, Ender
,
Gu, Shen
,
Coban-Akdemir, Zeynep
,
Posey, Jennifer E.
,
Bayram, Yavuz
,
Sutton, V. Reid
,
Carvalho, Claudia M.B.
,
Pehlivan, Davut
,
Gibbs, Richard A.
,
Lupski, James R.
Published in
HGG advances
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
5
Loading…
A novel homozygous mutation in ALS2 gene in four siblings with infantile-onset ascending hereditary spastic paralysis
by
Koçak Eker, Hatice
,
Ünlü, Süleyman Ersin
,
Al-Salmi, Fatema
,
Crosby, Andrew H
Published in
European journal of medical genetics
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
6
Loading…
Assessment of Pathogenic Variants in the PAH Gene and Genotype-Phenotype Correlation in Phenylketonuria Patients from Turkey
by
Balasar, Özgür
,
Kadıoğlu Yılmaz, Banu
,
Başdemirci, Müşerref
,
Koçak Eker, Hatice
,
Eser Çavdartepe, Büşra
,
Şimşek, Levent
,
Tunçez, Ebru
,
Duymuş, Fahrettin
Published in
Biochemical genetics
Get full text
Items that this one cites
Article
Save to List
Saved in:
7
Loading…
Cerebro-fronto-facial syndrome type 3 with polymicrogyria: A clinical presentation of Baraitser–Winter syndrome
by
Eker, Hatice Koçak
,
Derinkuyu, Betül Emine
,
Ünal, Sevim
,
Masliah-Planchon, Julien
,
Drunat, Séverine
,
Verloes, Alain
Published in
European journal of medical genetics
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
8
Loading…
Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases
by
Verloes, Alain
,
Di Donato, Nataliya
,
Masliah-Planchon, Julien
,
Jongmans, Marjolijn
,
Abdul-Raman, Omar A
,
Albrecht, Beate
,
Allanson, Judith
,
Brunner, Han
,
Bertola, Debora
,
Chassaing, Nicolas
,
David, Albert
,
Devriendt, Koen
,
Eftekhari, Pirayeh
,
Drouin-Garraud, Valérie
,
Faravelli, Francesca
,
Faivre, Laurence
,
Giuliano, Fabienne
,
Guion Almeida, Leina
,
Juncos, Jorge
,
Kempers, Marlies
,
Eker, Hatice Koçak
,
Lacombe, Didier
,
Lin, Angela
,
Mancini, Grazia
,
Melis, Daniela
,
Lourenço, Charles Marques
,
Siu, Victoria Mok
,
Morin, Gilles
,
Nezarati, Marjan
,
Nowaczyk, Malgorzata J M
,
Ramer, Jeanette C
,
Osimani, Sara
,
Philip, Nicole
,
Pierpont, Mary Ella
,
Procaccio, Vincent
,
Roseli, Zeichi-Seide
,
Rossi, Massimiliano
,
Rusu, Cristina
,
Sznajer, Yves
,
Templin, Ludivine
,
Uliana, Vera
,
Klaus, Mirjam
,
Van Bon, Bregje
,
Van Ravenswaaij, Conny
,
Wainer, Bruce
,
Fry, Andrew E
,
Rump, Andreas
,
Hoischen, Alexander
,
Drunat, Séverine
,
Rivière, Jean-Baptiste
,
Dobyns, William B
,
Pilz, Daniela T
Published in
European journal of human genetics : EJHG
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
9
Loading…
Whole-Exome Sequencing in Turkish Patients with Inherited Retinal Dystrophies Reveals Novel Variants in Ten Genes
by
Basdemirci, Muserref
,
Kocak Eker, Hatice
Published in
Molecular syndromology
Get full text
Article
Save to List
Saved in:
10
Loading…
A homozygous mutation in the POMT2 gene in four siblings with limb-girdle muscular dystrophy 2N
by
Yıldırım, Miraç
,
Koçak Eker, Hatice
,
Doğan, Melih Timuçin
Published in
Turkish archives of pediatrics
Get full text
Report
Save to List
Saved in:
Search Tools:
RSS Feed
Email Search
Save Search
Back
Refine Results
Page will reload when a filter is selected or excluded.
Limit To
Peer Reviewed
9 results
9
Full Text
10 results
10
Format
Articles
9 results
9
Reports
1 results
1
Journal Title
European Journal Of Medical Genetics
2 results
2
Biochemical Genetics
1 results
1
Child's Nervous System
1 results
1
European Journal Of Human Genetics : Ejhg
1 results
1
Hgg Advances
1 results
1
Journal Of Medical Virology
1 results
1
Molecular Syndromology
1 results
1
Turk Pediatri Arsivi
1 results
1
Turkish Archives Of Pediatrics
1 results
1
Subjects
Life Sciences & Biomedicine
9 results
9
Science & Technology
9 results
9
Genetics & Heredity
6 results
6
Female
4 results
4
Humans
4 results
4
Male
3 results
3
Mutation
3 results
3
Pediatrics
3 results
3
Abnormalities, Multiple - Diagnosis
2 results
2
Abnormalities, Multiple - Genetics
2 results
2
Actins - Genetics
2 results
2
Biochemistry & Molecular Biology
2 results
2
Case Report
2 results
2
Child
2 results
2
Child, Preschool
2 results
2
Craniofacial Abnormalities - Diagnosis
2 results
2
Craniofacial Abnormalities - Genetics
2 results
2
Dna Mutational Analysis
2 results
2
Medical Education
2 results
2
Patients
2 results
2
Year of Publication
From:
To:
Source
Free E-Journal (出版社公開部分のみ)
5 results
5
Pubmed (Medline)
5 results
5
Springer Link
3 results
3
Sciencedirect Journals
3 results
3
Doaj Directory Of Open Access Journals
3 results
3
Sciencedirect Freedom Collection 2022-2024
2 results
2
Road: Directory Of Open Access Scholarly Resources
2 results
2
Publicly Available Content Database (Proquest) (Pq Sdu P3)
2 results
2
Springer Nature - Connect Here First To Enable Access
2 results
2
Karger电子期刊和电子书数据库
2 results
2
Springer Link Contemporary
2 results
2
Wiley-Blackwell Journals
1 results
1
Wiley Online Library All Journals
1 results
1
Bacon - Elsevier - Global Sciencedirect-Openaccess
1 results
1
Wiley
1 results
1
Nature
1 results
1